المؤلفون: Gentilini, D, Muzza, M, de Filippis, T, Vigone, M C, Weber, G, Calzari, L, Cassio, A, Di Frenna, M, Bartolucci, M, Grassi, E S, Carbone, E, Olivieri, A, Persani, L

المساهمون: D. Gentilini, M. Muzza, T. de Filippi, M.C. Vigone, G. Weber, L. Calzari, A. Cassio, M. Di Frenna, M. Bartolucci, E.S. Grassi, E. Carbone, A. Olivieri, L. Persani

مصطلحات موضوعية: Congenital disease, Genome-wide DNA methylation, Preterm delivery, Thyroid, Thyroid dysgenesi, Twin gestation, Settore MED/13 - Endocrinologia

Relation: info:eu-repo/semantics/altIdentifier/pmid/36071330; info:eu-repo/semantics/altIdentifier/wos/WOS:000850744100002; volume:46; issue:2; firstpage:393; lastpage:404; numberofpages:12; journal:JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION; https://hdl.handle.net/2434/953214; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85137520724

الاتاحة: https://hdl.handle.net/2434/953214
https://doi.org/10.1007/s40618-022-01915-2

المؤلفون: Luca Persani

المساهمون: L. Persani

مصطلحات موضوعية: IQ, MRI, Thyroid dysgenesi, cognitive function, congenital hypothyroidism, Settore MED/13 - Endocrinologia

Relation: info:eu-repo/semantics/altIdentifier/pmid/34197588; info:eu-repo/semantics/altIdentifier/wos/WOS:000744541300041; journal:THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; http://hdl.handle.net/2434/857197; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85121261377

الاتاحة: http://hdl.handle.net/2434/857197
https://doi.org/10.1210/clinem/dgab487

المؤلفون: Rurale, Giuditta, Marelli, Federica, Duminuco, Paolo, Persani, Luca

المساهمون: G. Rurale, F. Marelli, P. Duminuco, L. Persani

مصطلحات موضوعية: congenital hypothyroidism, thyroid dysgenesi, endoderm, Sonic Hedgehog, thyroid development, zebrafish, Settore MED/13 - Endocrinologia, Settore BIO/13 - Biologia Applicata

Relation: info:eu-repo/semantics/altIdentifier/pmid/31797737; info:eu-repo/semantics/altIdentifier/wos/WOS:000509792100001; volume:30; issue:2; firstpage:277; lastpage:289; numberofpages:13; journal:THYROID; http://hdl.handle.net/2434/706228; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85080842945

الاتاحة: http://hdl.handle.net/2434/706228
https://doi.org/10.1089/thy.2019.0196

المؤلفون: VINCENZI, Monica, CAMILOT, Marta, Ferrarini, Eleonora, TEOFOLI, Francesca, VENTURI, Giacomo, GAUDINO, Rossella, CAVARZERE, Paolo, De Marco, Giuseppina, Agretti, Patrizia, Dimida, Antonio, Tonacchera, Massimo, BONER, Attilio, ANTONIAZZI, Franco

المساهمون: Vincenzi, Monica, Camilot, Marta, Ferrarini, Eleonora, Teofoli, Francesca, Venturi, Giacomo, Gaudino, Rossella, Cavarzere, Paolo, De Marco, Giuseppina, Agretti, Patrizia, Dimida, Antonio, Tonacchera, Massimo, Boner, Attilio, Antoniazzi, Franco

مصطلحات موضوعية: Biological Marker, Congenital Hypothyroidism, Female, Follow-Up Studie, Forkhead Transcription Factor, HEK293 Cell, Homeodomain Protein, Human, Hypothyroidism, Infant, Newborn, Male, Middle Aged, Nuclear Protein, Paired Box Transcription Factor, Pedigree, Prognosi, Promoter Regions, Genetic, Receptors, Thyrotropin, Thyroid Dysgenesi, Transcription Factors

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/25146893; info:eu-repo/semantics/altIdentifier/wos/WOS:000340955000001; volume:14; issue:1; firstpage:1; lastpage:7; numberofpages:7; journal:BMC ENDOCRINE DISORDERS; http://hdl.handle.net/11562/928890; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84906825748

الاتاحة: http://hdl.handle.net/11562/928890
https://doi.org/10.1186/1472-6823-14-69

المؤلفون: Riva, G, Villanova, M, Francia, G, Valotto, G, Mezzetto, L, TOAIARI, Marco, Eccher, A, Novelli, L

المساهمون: Riva, G, Villanova, M, Francia, G, Valotto, G, Mezzetto, L, Toaiari, Marco, Eccher, A, Novelli, L

مصطلحات موضوعية: Aberrant thyroid, Ectopic thyroid, Occult thyroid carcinoma, Ablation Technique, Aged, Choristoma, Diagnosis, Differential, Human, Lymphatic Metastasi, Male, Thyroid Cancer, Papillary, Thyroid Dysgenesi, Thyroid Gland, Thyroid Neoplasm, Ultrasonography

Relation: info:eu-repo/semantics/altIdentifier/pmid/30799444; info:eu-repo/semantics/altIdentifier/wos/WOS:000470010900005; volume:110; issue:4; firstpage:313; lastpage:315; numberofpages:3; journal:PATHOLOGICA; http://hdl.handle.net/11562/999237; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85062062280

الاتاحة: http://hdl.handle.net/11562/999237

المؤلفون: Paola Ungaro, Nicola Improda, Silvio Desiderio, Mariacarolina Salerno, Paolo Emidio Macchia, Vincenzo Cacace, Luigi Albano, A. Colao, Immacolata Cristina Nettore, E. De Nisco

المساهمون: Nettore, I. C., Desiderio, S., de Nisco, E., Cacace, V., Albano, L., Improda, N., Ungaro, P., Salerno, M., Colao, A., Macchia, P. E.

المصدر: Journal of endocrinological investigation (Testo stamp.) 41 (2018): 711–717. doi:10.1007/s40618-017-0795-7
info:cnr-pdr/source/autori:Nettore I.C.; Desiderio S.; De Nisco E.; Cacace V.; Albano L.; Improda N.; Ungaro P.; Salerno M.; Colao A.; Macchia P.E./titolo:High-resolution melting analysis (HRM) for mutational screening of Dnajc17 gene in patients affected by thyroid dysgenesis/doi:10.1007%2Fs40618-017-0795-7/rivista:Journal of endocrinological investigation (Testo stamp.)/anno:2018/pagina_da:711/pagina_a:717/intervallo_pagine:711–717/volume:41

مصطلحات موضوعية: 0301 basic medicine, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Thyroid Nuclear Factor 1, 030209 endocrinology & metabolism, Biology, Real-Time Polymerase Chain Reaction, medicine.disease_cause, Thyroid dysgenesis, High Resolution Melt, PAX8 Transcription Factor, 03 medical and health sciences, Exon, 0302 clinical medicine, Endocrinology, medicine, Humans, Allele, Child, thyroid dysgenesis, Genetics, Mutation, Thyroid, DNAJC17, Thyroid dysgenesi, HSP40 Heat-Shock Proteins, Prognosis, medicine.disease, Molecular biology, Congenital hypothyroidism, Phenotype, 030104 developmental biology, medicine.anatomical_structure, Female, PAX8, Biomarkers, Human

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a9e3e9ce4645b51dd123fde33adad77
http://www.cnr.it/prodotto/i/389708

المؤلفون: De Filippis, Tiziana, Marelli, Federica, Nebbia, Gabriella, Porazzi, Patrizia, Corbetta, Sabrina, Fugazzola, Laura, Gastaldi, Roberto, Vigone, Maria Cristina, Biffanti, Roberta, Frizziero, Daniela, Mandarã, Luana, Prontera, Paolo, Salerno, Mariacarolina, MAGHNIE, MOHAMAD, Tiso, Natascia, Radetti, Giorgio, Weber, Giovanna, Persani, Luca

المساهمون: De Filippis, Tiziana, Marelli, Federica, Nebbia, Gabriella, Porazzi, Patrizia, Corbetta, Sabrina, Fugazzola, Laura, Gastaldi, Roberto, Vigone, Maria Cristina, Biffanti, Roberta, Frizziero, Daniela, Mandarã , Luana, Prontera, Paolo, Salerno, Mariacarolina, Maghnie, Mohamad, Tiso, Natascia, Radetti, Giorgio, Weber, Giovanna, Persani, Luca

مصطلحات موضوعية: Adult, Alagille Syndrome, Animal, Calcium-Binding Protein, Child, Preschool, Computational Biology, Female, Fluorescent Antibody Technique, Human, Intercellular Signaling Peptides and Protein, Jagged-1 Protein, Male, Membrane Protein, Serrate-Jagged Protein, Thyroid Dysgenesi, Zebrafish, Zebrafish Protein, Endocrinology, Diabetes and Metabolism, Biochemistry, Clinical Biochemistry, Biochemistry (medical)

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/26760175; info:eu-repo/semantics/altIdentifier/wos/WOS:000378811300014; volume:101; firstpage:861; lastpage:870; numberofpages:10; journal:THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; http://hdl.handle.net/11567/876561; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84960866134

الاتاحة: http://hdl.handle.net/11567/876561
https://doi.org/10.1210/jc.2015-3403

المؤلفون: Paragliola, Rosa Maria, Papi, Giampaolo, Pontecorvi, Alfredo, Corsello, Salvatore Maria

المساهمون: Paragliola, Rosa Maria, Papi, Giampaolo, Lovicu, Rosa Maria, Pontecorvi, Alfredo, Corsello, Salvatore Maria

مصطلحات موضوعية: Female, Human, Hypothyroidism, Middle Aged, Submandibular Gland Disease, Thyroid Dysgenesi, Radiology, Nuclear Medicine and Imaging, Settore MED/13 - ENDOCRINOLOGIA

Relation: info:eu-repo/semantics/altIdentifier/pmid/27749423; info:eu-repo/semantics/altIdentifier/wos/WOS:000387999000015; volume:41; issue:12; firstpage:936-937; lastpage:937; issueyear:2016; journal:CLINICAL NUCLEAR MEDICINE; http://hdl.handle.net/10807/91865; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85028249724; http://journals.lww.com/nuclearmed/pages/default.aspx

الاتاحة: http://hdl.handle.net/10807/91865
https://doi.org/10.1097/RLU.0000000000001401
http://journals.lww.com/nuclearmed/pages/default.aspx

المؤلفون: Delvecchio, Maurizio, Salerno, Mariacarolina, Vigone, Maria Cristina, Wasniewska, Malgorzata, Popolo, Pietro Pio, Lapolla, Rosa, Tronconi, Giulia Maria, D’Acunzo, Ida, Di Mase, Raffaella, Falcone, Rosa Maria, Corrias, Andrea, De Luca, Filippo, Weber, Giovanna, Cavallo, Luciano, Faienza, Maria Felicia, MUSSA, ALESSANDRO

المساهمون: Delvecchio, Maurizio, Salerno, Mariacarolina, Vigone, Maria Cristina, Wasniewska, Malgorzata, Popolo, Pietro Pio, Lapolla, Rosa, Mussa, Alessandro, Tronconi, Giulia Maria, D’Acunzo, Ida, Di Mase, Raffaella, Falcone, Rosa Maria, Corrias, Andrea, De Luca, Filippo, Weber, Giovanna, Cavallo, Luciano, Faienza, Maria Felicia

مصطلحات موضوعية: Congenital hypothyroidism, Congenital hypothyroidism etiology, Congenital hypothyroidism severity, Replacement therapy, Thyroxine requirement, Female, Human, Infant, Newborn, Longitudinal Studie, Male, Thyroid Dysgenesi, Thyroxine, Endocrinology, Diabetes and Metabolism

Relation: info:eu-repo/semantics/altIdentifier/pmid/25762444; info:eu-repo/semantics/altIdentifier/wos/WOS:000370082400019; volume:50; issue:3; firstpage:674; lastpage:680; numberofpages:7; journal:ENDOCRINE; http://hdl.handle.net/2318/1614340; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84949102334; http://www.springer.com/humana+press/journal/12020

الاتاحة: http://hdl.handle.net/2318/1614340
https://doi.org/10.1007/s12020-015-0574-1
http://www.springer.com/humana+press/journal/12020

المؤلفون: BAGATTINI, BRUNELLA, Di Cosmo, Caterina, Montanelli, Lucia, Piaggi, Paolo, Ciampi, Mariella, Agretti, Patrizia, De Marco, Giuseppina, Vitti, Paolo, Tonacchera, Massimo

المساهمون: Bagattini, Brunella, Di Cosmo, Caterina, Montanelli, Lucia, Piaggi, Paolo, Ciampi, Mariella, Agretti, Patrizia, De Marco, Giuseppina, Vitti, Paolo, Tonacchera, Massimo

مصطلحات موضوعية: Adolescent, Adult, Congenital Hypothyroidism, Female, Hormone Replacement Therapy, Human, Hypothalamo-Hypophyseal System, Hypothyroidism, Male, Thyroid Dysgenesi, Thyroid Hormone Resistance Syndrome, Thyroid Hormone, Thyroidectomy, Thyroxine, Young Adult, Endocrinology, Diabetes and Metabolism

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/25305309; info:eu-repo/semantics/altIdentifier/wos/WOS:000344948400016; volume:171; issue:5; firstpage:615; lastpage:621; numberofpages:7; journal:EUROPEAN JOURNAL OF ENDOCRINOLOGY; http://hdl.handle.net/11568/956057; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84910140928; http://www.eje-online.org/content/171/5/615.full.pdf+html

الاتاحة: http://hdl.handle.net/11568/956057
https://doi.org/10.1530/EJE-14-0621
http://www.eje-online.org/content/171/5/615.full.pdf+html

المؤلفون: T. de Filippis, M. C. Vigone, M. Di Frenna, F. Marelli, G. Weber, L. Persani

المساهمون: T. de Filippi, F. Marelli, M.C. Vigone, M. Di Frenna, G. Weber, L. Persani

مصطلحات موضوعية: Brain-lung-thyroid syndrome, Choreoathetosi, Congenital hypothyroidism, NKX2-1, Thyroid dysgenesi, Thyroid ectopy, Settore MED/13 - Endocrinologia, Settore MED/38 - Pediatria Generale e Specialistica

Relation: volume:3; issue:4; firstpage:227; lastpage:233; numberofpages:7; journal:EUROPEAN THYROID JOURNAL; http://hdl.handle.net/2434/270642

الاتاحة: http://hdl.handle.net/2434/270642
https://doi.org/10.1159/000366274

المؤلفون: Ferrara AM, Rossi G, Zampella E, Di Candia S, Pagliara V, Nettore IC, Capalbo D, Baserga M, Salerno MC, Fenzi G, Macchia P.E., DE SANCTIS, Luisa

المساهمون: Ferrara AM, Rossi G, Zampella E, Di Candia S, Pagliara V, Nettore IC, Capalbo D, De Sanctis L, Baserga M, Salerno MC, Fenzi G, Macchia PE.

مصطلحات موضوعية: congenital hypothyroidism, thyroid dysgenesi, Transcription Factor

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/21060249; info:eu-repo/semantics/altIdentifier/wos/WOS:000295562600017; volume:34; issue:7; firstpage:149; lastpage:152; numberofpages:4; journal:JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION; http://hdl.handle.net/2318/108558; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84858779683

الاتاحة: http://hdl.handle.net/2318/108558
https://doi.org/10.3275/7331

المؤلفون: Ferrara AM, Rossi G, Capuano S, Del Prete G, Zampella E, Gianino P, Corrias A, Fenzi G, Zannini M, Macchia P.E., DE SANCTIS, Luisa

المساهمون: Ferrara AM, De Sanctis L, Rossi G, Capuano S, Del Prete G, Zampella E, Gianino P, Corrias A, Fenzi G, Zannini M, Macchia PE.

مصطلحات موضوعية: Congenital hypothyroidism, Thyroid development, Thyroid dysgenesi, Transcription factor, TAZ/WWTR1 gene, PAX8 gene

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/19542741; info:eu-repo/semantics/altIdentifier/wos/WOS:000267384900009; volume:32; issue:3; firstpage:238; lastpage:241; numberofpages:4; journal:JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION; http://hdl.handle.net/2318/108148; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-67651250122

الاتاحة: http://hdl.handle.net/2318/108148